Senior Statistician (RWE) Job at PHASTAR, United States

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  • PHASTAR
  • United States

Job Description

Overview

THE COMPANY

Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. With offices across the UK, US, Germany, Denmark, Kenya, Australia, India, China and Japan, Phastar is the second largest specialized biometrics provider globally, and the largest in the UK.

Our unique approach to data analysis, “The Phastar Discipline”, has led us to build a reputation for outstanding quality. With this as our core focus, we’re looking for talented individuals who share our passion for quality and technical expertise to join our team.

WHY PHASTAR

Accredited as an outstanding company to work for, Phastar is committed to employee engagement, workplace satisfaction and ensuring a healthy work-life balance. We offer flexible working, part-time hours, involvement in developing company-wide initiatives, structured training and development plans, and a truly supportive, fun and friendly environment.

What’s more, when you join our team, Phastar will plant a tree in your honour, as one of our Environmental, Social and Governance (ESG) initiatives. So, not only would you get your dream job, you’ll also be helping to save the planet!

THE ROLE

Work as a Senior Statistician on clinical trials; producing and validating complex outputs to excellent quality whilst adhering to deliverable timeline. Preparing randomization schedules and acting as the unblinded statistician on reporting teams. Contributing to the variety of RWE analytics studies: feasibility assessment, RWE studies, exploratory analysis. Act as a statistical consultant to pharmaceutical or biotech companies.



Responsibilities

Employees may be required to perform some or all of the following:

• Program and validate primary efficacy datasets
• Program and validate summary tables, listings and complex figures, program statistical analysis tables, according to the SAP, given specifications and pertinent study documentation Liaise with clients to propose alternatives or additional analyses if needed
• Develop macros for statistical analyses and figures
• Create, validate and QC of efficacy dataset specifications for single studies, ISS/ISEs, etc
• Write SAP text for any study
• Quality Control of TLF shells

• Contribute to the variety of RWE analytics studies: feasibility assessment, RWE studies, exploratory analysis

• Define the statistical analysis strategy for RWE studies using real world data available in house or through external collaboration

• Identify and contribute to the RWE analytics enabling projects, in order to improve execution of RWE studies: R code automatization, libraries of variables derivation, code lists

• Improve the data visualization for non-technical stakeholders
• Manage day-to-day workload to ensure project deliverables are met
• Awareness of CDISC standards

Qualifications

• PhD or MSc in Biostatistics or related discipline

• SAS, R simulations, Git experience is required

• Experience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation. Familiarity with GCP and regulatory requirements

APPLY NOW

With the world’s eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques. We offer flexible working, part-time hours, structured training and development plans, continuous learning opportunities, and a competitive salary and benefits package. We’re committed to ensuring our employees achieve a healthy work-life balance, within a supportive, fun and friendly working environment.

Should you feel that you have the right skill set and motivations for this position, please apply!

Phastar is committed to the principles and practices of equal opportunities and to encouraging the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, colour, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.

Important notice to Employment businesses/Agencies

Phastar does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Phastar's Head of Talent Acquisition to obtain prior written authorization before referring any candidates to Phastar. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Phastar. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Phastar. Phastar shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Job Tags

Permanent employment, Contract work, Part time, Flexible hours,

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